Canonical Allele Identifier: CA1619384428

Gene: SKIC2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31969627G= , CM000668.2:g.31969627G=	GRCh38
NC_000006.11:g.31937404G= , CM000668.1:g.31937404G=	GRCh37
NC_000006.10:g.32045383G=	NCBI36
NG_032652.1:g.15824G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.*2701G=	ENSP00000419905.1:n.*2701G=
ENST00000485349.6:n.4129G=
ENST00000491994.2:c.*195G=	ENSP00000417586.2:n.*195G=
ENST00000494058.6:n.3955G=
ENST00000697831.1:c.3584G=	ENSP00000513453.1:p.Gly1195=
ENST00000697832.1:n.3806G=
ENST00000697834.1:n.4371G=
ENST00000697835.1:c.*3171G=	ENSP00000513455.1:n.*3171G=
ENST00000697836.1:n.4007G=
ENST00000697837.1:c.*769G=	ENSP00000513456.1:n.*769G=
ENST00000697838.1:c.3518G=	ENSP00000513457.1:p.Gly1173=
ENST00000697839.1:n.4465G=
ENST00000697840.1:c.3689G=	ENSP00000513458.1:p.Gly1230=
ENST00000697841.1:n.4564G=
ENST00000697842.1:n.3908G=
ENST00000375394.7:c.3653G= MANE Select	ENSP00000364543.2:p.Gly1218=
ENST00000375394.6:c.3653G=	ENSP00000364543.2:p.Gly1218=
ENST00000465703.5:n.4383G=
ENST00000471818.1:n.582G=
ENST00000474839.5:c.*3025G=	ENSP00000420470.1:n.*3025G=
ENST00000483553.5:c.1183G=
ENST00000491994.1:c.742G=
NM_006929.4:c.3653G=	NP_008860.4:p.Gly1218=
XR_926301.3:n.3669G=
NM_006929.5:c.3653G= MANE Select	NP_008860.4:p.Gly1218=